A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10458n54



Internal ID20143882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31410991..31491965hg38UCSC Ensembl
chr6:31378768..31459742hg19UCSC Ensembl
chr6:31486747..31567721hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3880975
hg1980975
hg1880975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601925, nsv601924, nsv601926, nsv601928, nsv601927, nsv601929, nsv601931, nsv601933
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10458n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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